| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20917126-20917484 | Rare:128 | ||||
| chr22:20982170-20982322 | Common:2; Rare:40; Clinvar (benign):2 | ||||
| chr22:21002068-21002250 | Common:4; Rare:65 | ||||
| chr22:21867640-21867859 | Common:2; Rare:64 | ||||
| chr22:21937948-21938311 | Rare:112 | ||||
| chr22:23767925-23768031 | Rare:31 | ||||
| chr22:23857004-23857183 | Common:8; Rare:56 | ||||
| chr22:23857572-23857920 | Common:6; Rare:147 | ||||
| chr22:23894308-23894695 | Common:6; Rare:152 | ||||
| chr22:24011029-24011382 | Common:43; Rare:190 | ||||
| chr22:24245013-24245230 | Common:1; Rare:34 | ||||
| chr22:24270697-24270979 | Common:3; Rare:98 | ||||
| chr22:24555053-24555444 | Common:4; Rare:143 | ||||
| chr22:24555888-24556066 | Rare:51 | ||||
| chr22:25741861-25742239 | Common:2; Rare:84 |